Canonical Allele Identifier: CA1190288113
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114693374A= , CM000663.2:g.114693374A= GRCh38
NC_000001.10:g.115235995A= , CM000663.1:g.115235995A= GRCh37
NC_000001.9:g.115037518A= NCBI36
NG_008012.1:g.7182T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.22+2076T= ENSP00000358551.4:n.22+2076T=
ENST00000520113.7:c.34+62T= MANE Select ENSP00000430075.3:n.34+62T=
ENST00000637080.1:c.37+2063T= ENSP00000489753.1:n.37+2063T=
ENST00000369538.3:c.121+2076T= ENSP00000358551.3:n.121+2076T=
ENST00000520113.6:c.133+62T= ENSP00000430075.2:n.133+62T=
NM_000036.2:c.133+62T= NP_000027.2:n.133+62T=
NM_001172626.1:c.121+2076T= NP_001166097.1:n.121+2076T=
NM_000036.3:c.34+62T= MANE Select NP_000027.3:n.34+62T=
NM_001172626.2:c.22+2076T= NP_001166097.2:n.22+2076T=